Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149887719-149887808 | Rare:38 | ||||
chr1:149887833-149888236 | Rare:126 | ||||
chr1:149888338-149888671 | Common:4; Rare:81 | ||||
chr1:149899479-149899726 | Common:2; Rare:51 | ||||
chr1:149899794-149900070 | Common:1; Rare:71 | ||||
chr1:149917814-149917993 | Common:1; Rare:47 | ||||
chr1:149927729-149927999 | Common:2; Rare:101; Clinvar (benign):6 | ||||
chr1:149928187-149928393 | Common:2; Rare:43 | ||||
chr1:149937151-149937401 | Rare:44 | ||||
chr1:150010499-150010978 | Common:4; Rare:116 | ||||
chr1:150066922-150067058 | Common:1; Rare:23 | ||||
chr1:150067083-150067457 | Common:4; Rare:67 | ||||
chr1:150067517-150067840 | Common:1; Rare:77 | ||||
chr1:150149786-150150158 | Common:1; Rare:134 | ||||
chr1:150234641-150234933 | Rare:48 |